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Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma
dc.contributor.author | Mellid, Sara | |
dc.contributor.author | Gil, Eduardo | |
dc.contributor.author | Letón, Rocío | |
dc.contributor.author | Balbín Felechosa, Milagros | |
dc.date.accessioned | 2023-06-26T09:03:37Z | |
dc.date.available | 2023-06-26T09:03:37Z | |
dc.date.issued | 2023 | |
dc.identifier.citation | Frontiers in Endocrinology, 13 (2023); doi:10.3389/fendo.2022.1070074 | |
dc.identifier.issn | 1664-2392 | |
dc.identifier.uri | http://hdl.handle.net/10651/68631 | |
dc.description.sponsorship | Instituto de Salud Carlos III (ISCIII), through the "Acción Estratégica en Salud" (AES) [PI18/00454, PI20/01169]; European Regional Development Fund (ERDF); Spanish Ministry of Science, Innovation and Universities "Formación del Profesorado Universitario-FPU" fellowship [FPU19/04940] | |
dc.description.statementofresponsibility | Mellid S, Gil E, Letón R, Caleiras E, Honrado E, Richter S, Palacios N, Lahera M, Galofré JC, López-Fernández A, Calatayud M, Herrera-Martínez AD, Galvez MA, Matias-Guiu X, Balbín M, Korpershoek E, Lim ES, Maletta F, Lider S, Fliedner SMJ, Bechmann N, Eisenhofer G, Canu L, Rapizzi E, Bancos I, Robledo M, Cascón A | |
dc.language.iso | eng | |
dc.relation.ispartof | Frontiers in Endocrinology | |
dc.rights | © 2023 Los autores | |
dc.rights | CC Reconocimiento 4.0 Internacional | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | WOS:000932433800001 | |
dc.title | Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma | |
dc.type | journal article | |
dc.identifier.doi | 10.3389/fendo.2022.1070074 | |
dc.relation.projectID | ISCIII/PI18/00454 | |
dc.relation.projectID | ISCIII/PI20/01169 | |
dc.relation.publisherversion | http://dx.doi.org/10.3389/fendo.2022.1070074 | |
dc.rights.accessRights | open access | |
dc.type.hasVersion | VoR |
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